US20210077365A1 - Water-in-oil emulsion cosmetic - Google Patents

Water-in-oil emulsion cosmetic Download PDF

Info

Publication number
US20210077365A1
US20210077365A1 US16/620,284 US201816620284A US2021077365A1 US 20210077365 A1 US20210077365 A1 US 20210077365A1 US 201816620284 A US201816620284 A US 201816620284A US 2021077365 A1 US2021077365 A1 US 2021077365A1
Authority
US
United States
Prior art keywords
oil
cosmetic
water
mass
oil emulsion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
US16/620,284
Other languages
English (en)
Inventor
Marianne Ayaka TOUATI
Satoshi Yamaki
Yurika WATANABE
Takahiro KATORI
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shiseido Co Ltd filed Critical Shiseido Co Ltd
Assigned to SHISEIDO COMPANY, LTD. reassignment SHISEIDO COMPANY, LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WATANABE, Yurika, YAMAKI, SATOSHI, TOUATI, Marianne Ayaka, KATORI, Takahiro
Publication of US20210077365A1 publication Critical patent/US20210077365A1/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/064Water-in-oil emulsions, e.g. Water-in-silicone emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/062Oil-in-water emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25Silicon; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/365Hydroxycarboxylic acids; Ketocarboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/466Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4966Triazines or their condensed derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/602Glycosides, e.g. rutin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/895Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/965Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of inanimate origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41Particular ingredients further characterized by their size
    • A61K2800/412Microsized, i.e. having sizes between 0.1 and 100 microns
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/48Thickener, Thickening system

Definitions

  • the present invention relates to a water-in-oil emulsion cosmetic. More specifically, the present invention relates to a water-in-oil emulsion cosmetic in which the ultraviolet protection (blocking) effects are markedly improved by blending formulated amounts of a non-volatile polar oil and an oil phase thickener.
  • Sunscreen cosmetics which are a type of UV-care cosmetic, are cosmetics that are intended to protect the skin from damage due to ultraviolet rays by covering the skin with a coating film containing an ultraviolet absorbing agent or an ultraviolet scattering agent, thereby absorbing or scattering UVA and UVB rays and suppressing the amount of ultraviolet radiation that reaches the skin (Non-Patent Document 1).
  • sunscreen cosmetics are commonly obtained (provided) by blending an appropriate combination of ultraviolet absorbing agents that chemically absorb ultraviolet rays and ultraviolet scattering agents that physically reflect/scatter ultraviolet rays, in order to obtain a high SPF (Sun Protection Factor) value.
  • ultraviolet scattering agents represented by titanium oxide (dioxide) and zinc oxide, scatter visible light in addition to ultraviolet rays.
  • titanium oxide dioxide
  • zinc oxide scatter visible light in addition to ultraviolet rays.
  • the washability becomes poor.
  • the astringent effect of zinc oxide imparts a feeling of dryness to the skin and may cause the feeling in use to become worse.
  • Patent Document 1 proposes not-blending an ultraviolet scattering agent but blending a large amount of an ultraviolet absorbing agent, and meanwhile, blending in 0.5 to 2% by mass of a dextrin fatty acid ester and/or a sucrose fatty acid ester relative to the overall amount of the cosmetic in order to suppress oiliness and stickiness that occurs when increasing the amount of the ultraviolet absorbing agent.
  • Patent Document 1 JP 2011-126832 A
  • Non-Patent Document 1 Shin-keshohin-gaku [New Cosmetology], 2nd edition, edited by Takeo Mitsui, 2001, published by Nanzando, pp. 497-504
  • a purpose of the present invention is to provide a water-in-oil emulsion cosmetic that is able to provide sufficiently high ultraviolet protection (blocking) effects even without practically blending in any additional ultraviolet scattering agent.
  • the present inventors performed diligent investigations towards solving the aforementioned problem, as a result of which they discovered that high ultraviolet protection effects can be obtained, even when reducing the blended amount or not-blending an ultraviolet scattering agent, by using an ultraviolet absorbing agent in combination with a formulated amount of a non-volatile polar oil and an oil phase thickener, and accordingly, the present invention is complete.
  • the present invention provides a water-in-oil emulsion cosmetic comprising: (A) 6 to 40% by mass of an ultraviolet absorbing agent; (B) 15% by mass or more of a non-volatile polar ester oil (other than the (A) ultraviolet absorbing agent); and (C) 0.5 to 15% by mass of an oil phase thickener.
  • the present invention is able to provide excellent ultraviolet protection effects, even when practically no ultraviolet scattering agents are blended therein. For this reason, a cosmetic that does not result in unnatural whiteness and is versatile can be provided.
  • the water-in-oil emulsion cosmetic of the present invention is characterized by that containing (A) an ultraviolet absorbing agent, (B) a non-volatile polar oil, and (C) an oil phase thickener.
  • A an ultraviolet absorbing agent
  • B a non-volatile polar oil
  • C an oil phase thickener
  • component (A) ultraviolet absorbing agent blended in the water-in-oil emulsion cosmetic according to the present invention
  • component (A) ultraviolet absorbing agent blended in the water-in-oil emulsion cosmetic according to the present invention
  • component (A) it is possible to use one that is normally blended into sunscreen cosmetics.
  • the (A) ultraviolet absorbing agent is not particularly limited, but specific examples include organic ultraviolet absorbing agents such as ethylhexyl methoxycinnamate, octocrylene, 2-hydroxy-4-methoxybenzophenone, dimethicodiethylbenzalmalonate, t-butyl methoxydibenzoylmethane, ethylhexyl triazone, diethylamino hydroxybenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine, methylene bis-benzotriazolyl tetramethylbutylphenol, phenylbenzimidazole sulfonic acid, homosalate and ethylhexyl salicylate.
  • organic ultraviolet absorbing agents such as ethylhexyl methoxycinnamate, octocrylene, 2-hydroxy-4-methoxybenzophenone, dime
  • the blended amount of component (A) should be 6 to 40% by mass, more preferably 8 to 35% by mass, and even more preferably 10 to 30% by mass relative to the overall amount of the water-in-oil emulsion cosmetic. If the blended amount of component (A) is less than 6% by mass, sufficient ultraviolet protection effects cannot be obtained, and even if more than 40% by mass is blended, an increase in the ultraviolet protection effects that is commensurate with the blended amount cannot be expected, and this is undesirable for making the stability worse and the like.
  • Component (A) may be used as one kind alone or may be a combination of two or more types.
  • the (B) non-volatile polar oil (hereinafter sometimes referred to simply as “component (B)”) blended into the water-in-oil emulsion cosmetic according to the present invention is a polar ester oil that does not exhibit volatility at ambient temperature (25° C.) and ambient pressure (1 atm (9.8 ⁇ 10 4 Pa)) (for example, including oils having a boiling point equal to or higher than approximately 200° C. at ambient (atmospheric) pressure), and that has fluidity at ambient temperature and ambient (atmospheric) pressure.
  • the “polar oil” is not particularly limited as long as it is an oil having high polarity among oils that are generally used in cosmetics.
  • ultraviolet absorbing agent that may have ester bonds and be non-volatile and polar are counted as the component (A) in the present invention and are not included in component (B).
  • non-volatile polar oil examples include diisopropyl sebacate, isopropyl myristate, glyceryl tri-2-ethylhexanoate, cetyl 2-ethylhexanoate, tripropylene glycol dineopentanoate, isononyl isononanoate, cetyl octanoate, octyldodecyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, decyl oleate, hexyldecyl dimethyloctanoate, cetyl lactate, myristyl lactate, lanolin acetate, isocetyl stearate, isocetyl isostearate, cholesteryl 12-hydroxystearate, ethylene glycol di-2-ethylhexanoate, dipenta
  • the blended amount of component (B) should be 15% by mass or more, more preferably 18% by mass or more, and even more preferably 20% by mass or more relative to the overall amount of the water-in-oil emulsion cosmetic. If the blended amount of component (B) is less than 15% by mass, the ultraviolet protection effects cannot be sufficiently improved. On the other hand, if a large amount of component (B) is blended, there is a tendency for the feeling in use and the water resistance to become worse. Thus, at most, the blended amount should be 70% by mass or less and should more preferably be 50% by mass or less. Component (B) may be used as a single kind alone or as a combination of two or more kinds.
  • the (C) oil phase thickener (hereinafter sometimes referred to simply as “ingredient (C)”) blended in the water-in-oil emulsion cosmetic according to the present invention is a substance that can adjust the viscosity of the oil phase in the water-in-oil emulsion cosmetic.
  • component (C) dextrin fatty acid esters, sucrose fatty acid esters, fatty acids or salts thereof, hardened vegetable oils, solid or semi-solid vegetable oils, organically modified clay minerals, glyceryl fatty acid esters and amino acid-based gelling agents are preferred.
  • Dextrin fatty acid esters are esters of dextrin or reduced dextrin with a higher fatty acid, which may be used without any particular restrictions as long as they are generally used in cosmetics.
  • the dextrin or reduced dextrin one in which the average degree of sugar polymerization is 3 to 100 is preferably used.
  • a saturated fatty acid having 8 to 22 carbon atoms is preferably used as the constituent fatty acids in the dextrin fatty acid ester. Specific examples include dextrin palmitate, dextrin oleate, dextrin stearate, dextrin myristate, dextrin (palmitate/2-ethylhexanoate) and the like.
  • sucrose fatty acid ester (an alkyl chain of) the fatty acid is linear or branched, saturated or unsaturated chain having 12 to 22 carbon atoms is preferably used.
  • Specific examples include sucrose caprylic acid esters, sucrose capric acid esters, sucrose lauric acid esters, sucrose myristic acid esters, sucrose palmitic acid esters, sucrose stearic acid esters, sucrose oleic acid esters, sucrose erucic acid esters and the like.
  • the fatty acid may be solid at ambient temperature, and examples include myristic acid, palmitic acid, stearic acid, behenic acid and the like. Additionally, the fatty acid salt may be a calcium salt, a magnesium salt, an aluminum salt or the like of the above.
  • hardened vegetable oil examples include hardened palm kernel oil, hardened castor oil, hydrogenated peanut oil, hydrogenated rapeseed oil, hydrogenated palm oil, hydrogenated camellia oil, hydrogenated soybean oil, hydrogenated olive oil, hydrogenated macadamia nut oil, hydrogenated sunflower oil, hydrogenated wheat germ oil, hydrogenated rice germ oil, hydrogenated rice bran oil, hydrogenated cottonseed oil, hydrogenated avocado oil and the like.
  • a vegetable oil that is solid or semi-solid at room temperature it is also possible to use a vegetable oil that is solid or semi-solid at room temperature.
  • a solid oil refers to an oil that is solid at 25° C.
  • a semi-solid oil is in between solid and oil at 25° C. More specifically, one in which the melting point is within the range from 44° C. to 90° C., the viscosity measured with a B-type viscometer at 25° C. is 5000 mPa ⁇ s or higher, or furthermore, 10,000 mPa ⁇ s or higher, is preferred.
  • examples of vegetable oils that are solid or semi-solid at room temperature include cacao butter, coconut oil, palm oil, palm kernel oil, Japan tallow, shea butter and the like.
  • organically modified clay mineral it is possible to use a clay mineral modified by a quaternary ammonium salt type cationic surfactant, represented by the following general formula (1), which is a type of colloidal hydrated aluminum silicate having a three-layered structure.
  • a quaternary ammonium salt type cationic surfactant represented by the following general formula (1), which is a type of colloidal hydrated aluminum silicate having a three-layered structure.
  • X ⁇ Al, Fe(III), Mn(III) or Cr(III); Y ⁇ Mg, Fe(II), Ni, Zn or Li; and Z ⁇ K, Na or Ca.
  • the organically modified clay mineral can be obtained by treating, with a quaternary ammonium salt type cationic surfactant, a clay mineral which may be a natural or synthetic (in this case, an (OH) group in the formula is substituted with a fluorine) clay mineral in the montmorillonite group, such as montmorillonite, saponite or hectorite (commercial products include Veegum, Kunipia, Laponite, etc.), or a synthetic mica known under the name of sodium silicic mica or sodium or lithium taeniolite (commercial products include Dimonite, manufactured by Topy Industries, Ltd. etc.).
  • the quaternary ammonium salt type cationic surfactant used in this case is represented by the following general chemical formula (2):
  • R′ represents an alkyl group having 10 to 22 carbon atoms or a benzyl group
  • R 2 represents a methyl group or an alkyl group having 10 to 22 carbon atoms
  • R 3 and R 4 represent alkyl groups or hydroxyalkyl groups having 1 to 3 carbon atoms
  • X represents a halogen atom or a methylsulfate residue
  • Examples of the quaternary ammonium salt type cationic surfactant include dodecyltrimethylammonium chloride, myristyltrimethylammonium chloride, cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, arachyltrimethylammonium chloride, behenyltrimethylammonium chloride, myristyldimethylethylammonium chloride, cetyldimethylethylammonium chloride, stearyldimethylethylammonium chloride, arachyldimethylethylammonium chloride, behenyldimethylethylammonium chloride, myristyldiethylmethylammonium chloride, cetyldiethylmethylammonium chloride, stearyldiethylmethylammonium chloride, arachyldiethylmethylammonium chloride, behenyldiethylmethylammonium chloride, benz
  • organically modified clay minerals include dimethyl distearyl ammonium hectorite (distearyldimonium hectorite), dimethylalkylammonium hectorite, benzyldimethylstearylammonium hectorite, distearyldimethylammonium chloride-treated aluminum-magnesium silicate and the like. Of these, dimethyldistearylammonium hectorite is particularly preferred.
  • Bentone 27 (benzyldimethylstearylammonium chloride-treated hectorite, manufactured by Elementis Japan KK) and Bentone 38 (distearyldimethylammonium chloride-treated hectorite, manufactured by Elementis Japan KK) are preferred.
  • Glyceryl fatty acid esters are esterified reaction products obtained by reacting glycerin, a diprotic acid having 18 to 28 carbon atoms, and a fatty acid having 8 to 28 carbon atoms (excluding diprotic acids) and may be used without any particular restrictions as long as they are generally used in cosmetics. Specific examples include glyceryl (behenate/isostearate/eicosanedioate), glyceryl (behenate/eicosanedioate) and polyglyceryl-10 (behenate/eicosanedioate), etc.
  • amino acid-based gelling agents examples include dibutyl lauroyl glutamide, dibutyl ethylhexanoyl glutamide, polyamide-8, polyamide-3, N-lauroyl-L-glutamic acid dibutyl amide and the like.
  • the blended amount of component (C) should preferably be 0.5 to 15% by mass, more preferably 1 to 10% by mass, and even more preferably 1 to 8% by mass relative to the overall amount of the water-in-oil emulsion cosmetic. If the blended amount of component (C) is less than 0.5% by mass, then the ultraviolet protection effects cannot be sufficiently improved, and if more than 15% by mass is blended, then the viscosity becomes high, and this is undesirable in terms of the properties when used, such as by becoming difficult to spread over the skin. Additionally, component (C) may be one type used alone or may be a combination of two or more types. In particular, it is preferable for two or more types of oil phase thickeners to be blended, and for one of the types to be an organically modified clay mineral. Furthermore, it is preferable to blend 2% by mass or more of a (C) oil phase thickener other than an organically modified clay mineral.
  • the ultraviolet protection effects can be improved by containing the above-mentioned components (A) to (C).
  • component (D) a powder having an average particle size of 15 ⁇ m or smaller (hereinafter sometimes referred to simply as “component (D)”) in addition to the above-mentioned components (A) to (C).
  • component (D) a powder having an average particle size of 15 ⁇ m or smaller
  • Component (D) has an average particle size of 15 ⁇ m or smaller, more preferably 12 ⁇ m or smaller.
  • the lower limit of the average particle size is not particularly limited, it should preferably be 3 ⁇ m or larger for the reason that it becomes more difficult to handle and the like.
  • the average particle size can be measured by means of a laser diffraction/scattering method.
  • Component (D) used in the present invention is preferably selected from a group consisting of the following (i) to (iv):
  • Talc is a silicic acid salt-based clay mineral, which is widely used in cosmetics as an extender pigment in the same way as mica, sericite and the like.
  • hydrophobically treated talc wherein talc is the base material and the surface thereof is hydrophobically treated, is particularly preferred.
  • the hydrophobic treatment is not particularly restricted, but may, for example, be a silicone treatment (treatment with a silicone oil such as methylhydrogen polysiloxane, dimethyl polysiloxane or methylphenyl polysiloxane; an alkylsilane such as methyltrimethoxysilane, ethyltrimethoxysilane, hexyltrimethoxysilane or octyltrimethoxysilane; or a fluoroalkylsilane such as trifluoromethylethyl trimethoxysilane or heptadecafluorodecyl trimethoxysilane), a fatty acid treatment (treatment with palmitic acid, isostearic acid, stearic acid, lauric acid, myristic acid, behenic acid, oleic acid, rosin acid, 12-hydroxystearic acid or the like), a fatty acid soap treatment (treatment with aluminum stearate, calcium
  • hydrophobically treated talc it is possible to use a commercial product, an example of which is “Calcium stearate-treated talc” (Fujimoto Chemicals Co., Ltd.).
  • silicone powder one that is normally used as a cosmetic raw material may be used.
  • silicone powders methylpolysiloxane network polymers, crosslinked methylpolysiloxane, crosslinked silicone-network silicone block copolymers, silylated silica and the like are known. Of these, crosslinked silicone-network silicone block copolymers are particularly preferred.
  • silicone powder commercial product that can be used is “KSP-100” (manufactured by Shin-etsu Chemical Co., Ltd. (vinyl dimethicone/methicone silsesquioxane) crosspolymer, average particle size 5 ⁇ m).
  • PMMA powder any type that is normally used as a cosmetic raw material may be used, as long as the average particle size is 15 ⁇ m or smaller.
  • crosslinked poly(methyl methacrylate) powder it is possible to use a commercial product, an example of which is “Ganzpearl” (manufactured by Aica Kogyo Co., Ltd., average particle size 8 ⁇ m).
  • silica silicic anhydride
  • any type that is normally used as a cosmetic raw material may be used, regardless of whether it is porous or non-porous.
  • Examples of commercial products include “Sunsphere H-31” (manufactured by AGC Si-Tech Co., Ltd.) (average particle size 3 ⁇ m), “Sunsphere H-51” (manufactured by AGC Si-Tech Co., Ltd.) (average particle size 5 ⁇ m) and “Sunsphere H-121” (manufactured by AGC Si-Tech Co., Ltd.) (average particle size 12 ⁇ m).
  • silica having a hydrophobically treated surface such as, for example, dimethylsilylated silicic anhydride and trimethylsilylated silicic anhydride.
  • the component (D) selected from the above-mentioned (i) to (iv) may be of one type used alone or may be a combination of two or more types.
  • the blended amount of component (D) is not particularly limited, but should preferably be 1 to 30% by mass, more preferably 1 to 25% by mass, and even more preferably 1 to 20% by mass relative to the overall amount of the water-in-oil emulsion cosmetic. If the blended amount of component (D) is less than 1% by mass, then there is a tendency for the effects of component (D) to not be able to be sufficiently obtained. If more than 30% by mass is blended, then there are cases in which the properties when used become worse, such as squeakiness, smudges and stickiness occurring, and cases in which the cosmetic becomes difficult to formulate.
  • the water-in-oil emulsion cosmetic of the present invention is able to realize sufficient ultraviolet protection effects by containing the above-mentioned components (A) to (C), even without blending in an ultraviolet scattering agent.
  • an ultraviolet scattering agent for the purpose of further improving the protection effects against ultraviolet rays.
  • it should be 6% by mass or less, preferably 5% by mass or less, more preferably 4% by mass or less, and particularly preferably 3% by mass or less relative to the overall amount of the water-in-oil emulsion cosmetic in order to suppress unnatural whiteness and reductions of the texture due to the ultraviolet scattering agent.
  • the ultraviolet scattering agent that may be blended in the water-in-oil emulsion cosmetic of the present invention is not particularly limited, and an ultraviolet scattering agent that is normally used in cosmetics may be used.
  • ultraviolet scattering agents include fine-particle metal oxides such as zinc oxide, titanium oxide, iron oxide, cerium oxide and tungsten oxide, and these metal oxides with surfaces that have been subjected to various hydrophobic surface treatments.
  • hydrophobic surface treatment agent that is generally used in the cosmetic field including, for example, silicones such as dimethicone and alkyl-modified silicone, alkoxysilanes such as octyltriethoxysilane, dextrin fatty acid esters such as dextrin palmitate, and fatty acids such as stearic acid may be used.
  • silicones such as dimethicone and alkyl-modified silicone
  • alkoxysilanes such as octyltriethoxysilane
  • dextrin fatty acid esters such as dextrin palmitate
  • fatty acids such as stearic acid
  • the water-in-oil emulsion cosmetic of the present invention may appropriately contain, as needed, components that are normally used in cosmetics such as, for example, oils, water, alcohols, surfactants, oil-based active agents, water-based active agents, water phase thickeners, humectants and antioxidants.
  • components that are normally used in cosmetics such as, for example, oils, water, alcohols, surfactants, oil-based active agents, water-based active agents, water phase thickeners, humectants and antioxidants.
  • a surfactant that may be used in the present invention is preferably a surfactant having an HLB lower than 8, particularly a silicon-based surfactant, in order to obtain a water-in-oil emulsion state.
  • silicone-based surfactants having an HLB lower than 8 include polyoxyalkylene-modified silicones, polyoxyalkylene/alkyl co-modified silicones, polyglycerin-modified silicones and/or polyglycerin/alkyl co-modified silicones.
  • KF-6017 PEG-10 dimethicone, manufactured by Shin-etsu Chemical Co., Ltd.
  • KF-6028 PEG-9 polydimethylsiloxyethyl dimethicone, manufactured by Shin-etsu Chemical Co., Ltd.
  • ABIL EM 90 cetyl PEG/PPG-10/1 dimethicone, manufactured by Evonik Goldschmidt Corp.
  • KF-6038 laauryl PEG-9 polydimethylsiloxyethyl dimethicone, manufactured by Shin-etsu Chemical Co., Ltd.
  • the blended amount of the silicone-based surfactant should preferably be 0.1 to 8% by mass, more preferably 0.2 to 7% by mass, even more preferably 0.4 to 5% by mass relative to the overall amount of the water-in-oil emulsion cosmetic.
  • the water-in-oil emulsion cosmetic of the present invention may be provided not only, for example, as a sunscreen cream, a sunscreen milky lotion or a sunscreen lotion, but may also be used as a foundation, a makeup base, a makeup cosmetic, a hair cosmetic or the like imparted with sunscreen effects, and may be produced by a conventional method.
  • Water-in-oil emulsion cosmetics having the compositions indicated in Tables 1 and 2 below were prepared by heating and melting the oil-based components and dispersing the powder therein, adding the separately mixed water phase thereto, and emulsifying the mixture by stirring.
  • T transmittance of sample
  • To transmittance of uncoated plate
  • the water-in-oil emulsion cosmetics having the compositions indicated in Table 3 below were prepared in the same manner as above, and the ultraviolet protection effects were evaluated by measuring the in-vitro SPF of the cosmetics by the method indicated below.
  • Water-in-oil emulsion cosmetics having the compositions indicated in Table 4 and Table 5 below were prepared, and the cumulative absorbance (Abs) values were measured in the same manner as above.
  • Crosslinked silicone-network silicone — 10 — — — — — — — — block copolymer (30 ⁇ m) Calcium stearate-treated talc (average — — — 10 — — — particle size 7 ⁇ m)
  • Crosslinked silicone-network silicone — — — — — 10 — — block copolymer (5 ⁇ m)
  • Silicic anhydride (average particle size 5 — — — — — — 10 ⁇ m)
  • Calcium stearate-treated talc (average particle 10 — — — — — size 22 ⁇ m) Dimethylpolysiloxane-treated talc (average — 10 — — — — particle size 12 ⁇ m) Perfluorooctyltriethoxysilane/alkyl acrylate — — 10 — — — — copolymer methyl polysiloxane ester-treated talc (average particle size 12 ⁇ m) Carboxydecyltrisiloxane zinc salt-treated talc — — — 10 — — (average particle size 12 ⁇ m) Triethoxysilylethyl polydimethylsiloxyethyl — — — 10 — hexyl dimethicone-treated talc (average particle size 12 ⁇ m) Triethoxysilylethyl polydimethylsiloxyethyl — — — — 10 —
  • Blended amount (Component Name) (% by mass) Purified water balance Alcohol 5 Trisodium 0.1 edetate Table salt 0.1 Sodium 0.01 pyrosulfite Phenoxyethanol 1 Glycerin 5 Erythritol 1 Xylitol 1 Tormentilia 0.1 extract Sodium hyaluronate 0.1 2-O-ethyl L-ascorbic acid 0.1 Dipotassium 0.05 glycyrrhizinate Isopropyl myristate 5 Glyceryl tri-2-ethylhexanoate 5 Diisopropyl sebacate 5 Alkyl (C 12-15 ) benzoate 3 Methyl polysiloxane 6 Cyclopentasiloxane 6 50% Trisiloxysilicic acid in 2 cyclopentasiloxane solution Dextrin palmitate 2 2-Ethylhexyl methoxycinnamate 5 Homosalate 5 Hydrophobically treated fine-particle 3 titanium
  • Crosslinked silicone-network silicone 6 block copolymer (average particle size 5 ⁇ m) Fine-particle dimethylsilylated silica 0.5 Lauryl PEG-9 2 polydimethylpolysiloxyethyl dimethicone Dimethyl distearyl 1 ammonium hectorite Dextrin palmitate 0.5 Isostearic acid 0.2 Tocopherol 0.01 Fragrance s.a.
  • Blended amount (Component Name) (% by mass) Purified water balance Alcohol 10 Trisodium 0.1 edetate Table salt 0.1 Sodium 0.01 pyrosulfite Glycerin 1 Xylitol 1 Tormentilla 0.1 extract Sodium 0.1 hyaluronate 2-O-ethyl L-ascorbic acid 0.1 Dipotassium 0.05 glycyrrhizinate Isododecane 5 Diisopropyl sebacate 8 Glyceryl tri-2-ethylhexanoate 5 Isopropyl myristate 5 PBG/PPG-9/1 copolymer 2 Methyl polysiloxane 5 Cyclopentasiloxane 3 Caprylyl methicone 3 20% Highly polymerized aminopropyl 1 dimethicone in dimethicone 20 cs solution 50% Trifluoroalkyl dimethyl 3 trimethylsiloxysilicic acid dimethicone solution Dextrin palm
  • Blended amount (Component Name) (% by mass) Purified water balance Alcohol 8 Trisodium 0.2 edetate Silica 0.5 Glycerin 1 Polyoxyethylene (14) 1 polyoxypropylene (7) dimethyl ether Rosa canina fruit oil 0.1 Sodium 0.1 hyaluronate 2-O-ethyl L-ascorbic acid 0.5 Dipotassium 0.05 glycyrrhizinate Isododecane 10 Glyceryl tri-2-ethylhexanoate 5 Isopropyl myristate 5 Diisopropyl sebacate 5 Alkyl (C 12-15 ) benzoate 3 PBG/PPG-9/1 copolymer 1 Methyl polysiloxane 10 Cyclopentasiloxane 3 50% Trisiloxysilicic acid 0.5 in cyclopentasiloxane solution Sucrose tetrastearate triacetate 1 Dextrin palmitate 2 2-Ethylhexyl

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Emergency Medicine (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Inorganic Chemistry (AREA)
  • Dermatology (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)
US16/620,284 2017-06-08 2018-06-06 Water-in-oil emulsion cosmetic Pending US20210077365A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2017-113231 2017-06-08
JP2017113231 2017-06-08
PCT/JP2018/021662 WO2018225768A1 (fr) 2017-06-08 2018-06-06 Préparation cosmétique de type émulsion eau-dans-l'huile

Publications (1)

Publication Number Publication Date
US20210077365A1 true US20210077365A1 (en) 2021-03-18

Family

ID=64566706

Family Applications (1)

Application Number Title Priority Date Filing Date
US16/620,284 Pending US20210077365A1 (en) 2017-06-08 2018-06-06 Water-in-oil emulsion cosmetic

Country Status (7)

Country Link
US (1) US20210077365A1 (fr)
EP (1) EP3636245A4 (fr)
JP (2) JP7295797B2 (fr)
KR (1) KR102648547B1 (fr)
CN (1) CN110785160A (fr)
TW (1) TW201902454A (fr)
WO (1) WO2018225768A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4245291A1 (fr) * 2022-03-17 2023-09-20 Symrise AG Additif pour écrans solaires
EP4245292A1 (fr) * 2022-03-17 2023-09-20 Symrise AG Additif pour écrans solaires
WO2023175129A1 (fr) 2022-03-17 2023-09-21 Symrise Ag Additif pour écrans solaires

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7240857B2 (ja) * 2018-11-15 2023-03-16 ポーラ化成工業株式会社 油中水型乳化組成物
CN114340583A (zh) * 2019-09-05 2022-04-12 株式会社资生堂 油包水型组合物
CN114599340B (zh) 2019-10-30 2024-04-30 陶氏环球技术有限责任公司 具有中空介孔二氧化硅纳米球的防晒组合物
CN114828809A (zh) * 2019-12-16 2022-07-29 株式会社资生堂 防晒化妆品

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3561999A (en) * 1967-12-06 1971-02-09 Huber Corp J M Metallic stearate coated clays and the process of producing same
US6485713B1 (en) * 2002-03-05 2002-11-26 The C. P. Hall Company Sunscreen compositions and methods and materials for producing the same
US20050118210A1 (en) * 2002-01-15 2005-06-02 Hisanori Kachi Water-in-oil emulsion preparation for external use on skin
US20080233060A1 (en) * 2007-03-19 2008-09-25 Grune Guerry L High SPF transparent or translucent, cytoprotective, biodegradable, UV radiation resistant compositions
US7501136B2 (en) * 2003-09-30 2009-03-10 Kao Corporation Deodorant composition
US20100008875A1 (en) * 2007-02-23 2010-01-14 Shiseido Company Ltd. Composition For Skin Or Hair
US20100055139A1 (en) * 2008-09-03 2010-03-04 Wilson Lee Compositions Comprising Solid Particles Encapsulated In A Cross-Linked Silicone Matrix, And Methods Of Making The Same
US20100092408A1 (en) * 2008-10-14 2010-04-15 Laurie Ellen Breyfogle Resilient personal care composition comprising polyalkyl ether containing siloxane elastomers
US20100166684A1 (en) * 2008-12-25 2010-07-01 Kokyu Alcohol Kogyo Co., Ltd. Water-in-oil type emulsified cosmetic
US20110182846A1 (en) * 2007-08-10 2011-07-28 Shiseido Company Ltd. Surface Treating Agent, Surface-Treated Powder, And Cosmetic
US20120288458A1 (en) * 2010-01-26 2012-11-15 Shiseido Company, Ltd. Water-In-Oil Emulsion Sunscreen Cosmetic Composition
JP2013199443A (ja) * 2012-03-23 2013-10-03 Mandom Corp 水中油型乳化組成物
WO2016017188A2 (fr) * 2015-08-03 2016-02-04 Shiseido Company, Ltd. Produit cosmétique solide sous forme d'émulsion eau dans l'huile
WO2016068300A1 (fr) * 2014-10-31 2016-05-06 株式会社 資生堂 Produit cosmétique de protection solaire
JP2016098178A (ja) * 2014-11-18 2016-05-30 株式会社ファンケル 日焼け止め化粧料
WO2018179451A1 (fr) * 2017-03-30 2018-10-04 日光ケミカルズ株式会社 Produit cosmétique en émulsion de type huile dans eau

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3604247B2 (ja) * 1996-12-18 2004-12-22 株式会社ノエビア 油中水型乳化化粧料
JP4011799B2 (ja) 1999-08-19 2007-11-21 株式会社資生堂 日焼け止め化粧料
JP3781994B2 (ja) * 2001-10-11 2006-06-07 株式会社トキワ 固型粉末化粧料
KR101371808B1 (ko) * 2006-02-20 2014-03-07 가부시키가이샤 시세이도 유중수형 유화 선스크린 화장료
JP5083801B2 (ja) * 2006-02-20 2012-11-28 株式会社 資生堂 油中水型乳化日焼け止め化粧料
JP2009007571A (ja) * 2007-05-31 2009-01-15 Pentel Corp 油性インキ
JP5295534B2 (ja) * 2007-09-10 2013-09-18 株式会社 資生堂 日焼け止め油中水型乳化化粧料
JP2011126832A (ja) 2009-12-18 2011-06-30 Shiseido Co Ltd 油中水型乳化日焼け止め化粧料
JP5723359B2 (ja) * 2010-03-24 2015-05-27 株式会社 資生堂 日焼け止め化粧料
JP5546056B2 (ja) * 2011-08-31 2014-07-09 株式会社 資生堂 油中水型乳化日焼け止め化粧料
JP6438409B2 (ja) * 2012-12-18 2018-12-12 ロレアル 化粧用光防護組成物
JP6130203B2 (ja) * 2013-04-26 2017-05-17 花王株式会社 皮膚化粧料
WO2014203913A1 (fr) * 2013-06-18 2014-12-24 L'oreal Composition cosmétique
JP6246614B2 (ja) * 2014-02-20 2017-12-13 日本メナード化粧品株式会社 油性固形口唇化粧料
BR112017008815A2 (pt) * 2014-10-31 2018-03-27 Shiseido Co Ltd cosmético protetor solar de emulsão água em óleo.
WO2017057676A1 (fr) * 2015-09-30 2017-04-06 株式会社 資生堂 Produit cosmétique d'écran solaire
WO2017057675A1 (fr) * 2015-09-30 2017-04-06 株式会社 資生堂 Cosmétique d'écran solaire
JP6263244B2 (ja) 2015-10-09 2018-01-17 株式会社 資生堂 噴霧型日焼け止め化粧料

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3561999A (en) * 1967-12-06 1971-02-09 Huber Corp J M Metallic stearate coated clays and the process of producing same
US20050118210A1 (en) * 2002-01-15 2005-06-02 Hisanori Kachi Water-in-oil emulsion preparation for external use on skin
US6485713B1 (en) * 2002-03-05 2002-11-26 The C. P. Hall Company Sunscreen compositions and methods and materials for producing the same
US7501136B2 (en) * 2003-09-30 2009-03-10 Kao Corporation Deodorant composition
US20100008875A1 (en) * 2007-02-23 2010-01-14 Shiseido Company Ltd. Composition For Skin Or Hair
US20080233060A1 (en) * 2007-03-19 2008-09-25 Grune Guerry L High SPF transparent or translucent, cytoprotective, biodegradable, UV radiation resistant compositions
US20110182846A1 (en) * 2007-08-10 2011-07-28 Shiseido Company Ltd. Surface Treating Agent, Surface-Treated Powder, And Cosmetic
US20100055139A1 (en) * 2008-09-03 2010-03-04 Wilson Lee Compositions Comprising Solid Particles Encapsulated In A Cross-Linked Silicone Matrix, And Methods Of Making The Same
US20100092408A1 (en) * 2008-10-14 2010-04-15 Laurie Ellen Breyfogle Resilient personal care composition comprising polyalkyl ether containing siloxane elastomers
US20100166684A1 (en) * 2008-12-25 2010-07-01 Kokyu Alcohol Kogyo Co., Ltd. Water-in-oil type emulsified cosmetic
US20120288458A1 (en) * 2010-01-26 2012-11-15 Shiseido Company, Ltd. Water-In-Oil Emulsion Sunscreen Cosmetic Composition
JP2013199443A (ja) * 2012-03-23 2013-10-03 Mandom Corp 水中油型乳化組成物
WO2016068300A1 (fr) * 2014-10-31 2016-05-06 株式会社 資生堂 Produit cosmétique de protection solaire
JP2016098178A (ja) * 2014-11-18 2016-05-30 株式会社ファンケル 日焼け止め化粧料
WO2016017188A2 (fr) * 2015-08-03 2016-02-04 Shiseido Company, Ltd. Produit cosmétique solide sous forme d'émulsion eau dans l'huile
WO2018179451A1 (fr) * 2017-03-30 2018-10-04 日光ケミカルズ株式会社 Produit cosmétique en émulsion de type huile dans eau
US20200030201A1 (en) * 2017-03-30 2020-01-30 Nikko Chemicals Co., Ltd. Oil-in-water emulsion cosmetic

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
Antoniou et al. "Sunscreens – what’s important to know," JEADV 22:1110-1119, 2008 (Year: 2008) *
Google translation JP 2013-199433 A, printed 2023 (Year: 2023) *
ip.com translation JP 2016-098178 A, printed 2024 (Year: 2024) *
O’Lenick et al. "The effects of solvents on sunscreens: a new ester to improve efficiency," 2013; https://www.cosmeticsandtoiletries.com/formulas-products/sun-care/article/21837011/the-effects-of-solvents-on-sunscreens-a-new-ester-to-improve-efficiency (Year: 2013) *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4245291A1 (fr) * 2022-03-17 2023-09-20 Symrise AG Additif pour écrans solaires
EP4245292A1 (fr) * 2022-03-17 2023-09-20 Symrise AG Additif pour écrans solaires
WO2023175129A1 (fr) 2022-03-17 2023-09-21 Symrise Ag Additif pour écrans solaires

Also Published As

Publication number Publication date
CN110785160A (zh) 2020-02-11
JPWO2018225768A1 (ja) 2020-04-09
JP2023089269A (ja) 2023-06-27
KR102648547B1 (ko) 2024-03-18
KR20200014313A (ko) 2020-02-10
EP3636245A4 (fr) 2021-03-10
TW201902454A (zh) 2019-01-16
JP7295797B2 (ja) 2023-06-21
WO2018225768A1 (fr) 2018-12-13
EP3636245A1 (fr) 2020-04-15

Similar Documents

Publication Publication Date Title
EP3213742B1 (fr) Produit cosmétique de protection solaire sous forme d'émulsion eau-dans-huile
JP7295797B2 (ja) 油中水型乳化化粧料
JP6535329B2 (ja) 水中油型乳化組成物
EP3360534B1 (fr) Produit cosmétique d'écran solaire pouvant être pulvérisé
KR100621383B1 (ko) 선스크린 조성물
JP4866066B2 (ja) 化粧料
JP2017122075A (ja) 水中油型皮膚化粧料
JP2023054249A (ja) 油中水型乳化化粧料
JP7347993B2 (ja) 日焼け止め用組成物
JP6831737B2 (ja) 水中油型化粧料
JP2019202962A (ja) アクリル系ポリマー含有ピッカリングエマルション
US20240148616A1 (en) Water-in-oil emulsion composition, cosmetic, and method for preparing water-in-oil emulsion composition
TWI828835B (zh) 皮膚外用劑
WO2022239842A1 (fr) Agent à usage externe pour la peau
WO2021100676A1 (fr) Préparation externe pour la peau
WO2024116839A1 (fr) Produit cosmétique de soin solaire à phase unique
TW202037362A (zh) 外用劑

Legal Events

Date Code Title Description
AS Assignment

Owner name: SHISEIDO COMPANY, LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TOUATI, MARIANNE AYAKA;YAMAKI, SATOSHI;WATANABE, YURIKA;AND OTHERS;SIGNING DATES FROM 20191220 TO 20200114;REEL/FRAME:051652/0750

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED